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神经生长因子对诱导多能干细胞软骨形成过程中软骨纤维化和肥大的影响

The Effect of Nerve Growth Factor on Cartilage Fibrosis and Hypertrophy during Chondrogenesis Using Induced Pluripotent Stem Cells.

作者信息

Jung Se In, Choi Si Hwa, Kim Jang-Woon, Lim Jooyoung, Rim Yeri Alice, Ju Ji Hyeon

机构信息

Catholic iPSCs Research Center, CiSTEM Laboratory, Department of Medical Sciences, Graduate School The Catholic University of Korea, Seoul, Korea.

Department of Medical Sciences, Graduate School of The Catholic University of Korea, Seoul, Korea.

出版信息

Int J Stem Cells. 2025 Feb 28;18(1):59-71. doi: 10.15283/ijsc24097. Epub 2024 Dec 30.

Abstract

Nerve growth factor (NGF) is a neurotrophic factor usually involved in the survival, differentiation, and growth of sensory neurons and nociceptive function. Yet, it has been suggested to play a role in the pathogenesis of osteoarthritis (OA). Previous studies suggested a possible relationship between NGF and OA; however, the underlying mechanisms remain unknown. Therefore, we investigated the impact of NGF in chondrogenesis using human induced pluripotent stem cells (hiPSCs)-derived chondrogenic pellets. To investigate how NGF affects the cartilage tissue, hiPSC-derived chondrogenic pellets were treated with NGF on day 3 of differentiation, expression of chondrogenic, hypertrophic, and fibrotic markers was confirmed. Also, inflammatory cytokine arrays were performed using the culture medium of the NGF treated chondrogenic pellets. As a result, NGF treatment decreased the expression of pro-chondrogenic markers by approximately 2~4 times, and hypertrophic (pro-osteogenic) markers and fibrotic markers were increased by approximately 3-fold or more in the NGF-treated cartilaginous pellets. In addition, angiogenesis was upregulated by approximately 4-fold or more, bone formation by more than 2-fold, and matrix metalloproteinase induction by more than 2-fold. These inflammatory cytokine array were using the NGF-treated chondrogenic pellet cultured medium. Furthermore, it was confirmed by Western blot to be related to the induction of the glycogen synthase kinase-3 beta (GSK3β) pathway by NGF. In Conclusions, these findings provide valuable insights into the multifaceted role of NGF in cartilage hypertrophy and fibrosis, which might play a critical role in OA progression.

摘要

神经生长因子(NGF)是一种神经营养因子,通常参与感觉神经元的存活、分化和生长以及伤害感受功能。然而,有人提出它在骨关节炎(OA)的发病机制中起作用。先前的研究表明NGF与OA之间可能存在关联;然而,其潜在机制仍不清楚。因此,我们使用人诱导多能干细胞(hiPSC)来源的软骨生成微球研究了NGF在软骨生成中的影响。为了研究NGF如何影响软骨组织,在分化第3天用NGF处理hiPSC来源的软骨生成微球,确认软骨生成、肥大和纤维化标志物的表达。此外,使用经NGF处理的软骨生成微球的培养基进行炎症细胞因子阵列分析。结果,NGF处理使促软骨生成标志物的表达降低了约2至4倍,在经NGF处理的软骨微球中,肥大(促骨生成)标志物和纤维化标志物增加了约3倍或更多。此外,血管生成上调了约4倍或更多,骨形成上调了2倍以上,基质金属蛋白酶诱导上调了2倍以上。这些炎症细胞因子阵列分析使用的是经NGF处理的软骨生成微球培养基。此外,通过蛋白质免疫印迹法证实这与NGF诱导糖原合酶激酶-3β(GSK3β)途径有关。总之,这些发现为NGF在软骨肥大和纤维化中的多方面作用提供了有价值的见解,这可能在OA进展中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/feb7/11867901/9b3d99009a81/ijsc-18-1-59-f1.jpg

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